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Mol Cell Biol, June 1998, p. 3604-3611, Vol. 18, No. 6
Department of Biochemistry and the Vanderbilt
Cancer Center, Vanderbilt University School of Medicine, Nashville,
Tennessee 37027,1 and
Department of
Pharmaceutical Science, St. Jude Children's Research Hospital,
Memphis, Tennessee 381052
Received 2 December 1997/Returned for modification 20 February
1998/Accepted 24 March 1998
Chromosomal translocations in acute leukemia that affect the
AML-1/CBF
0270-7306/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
The MYND Motif Is Required for Repression of Basal
Transcription from the Multidrug Resistance 1 Promoter by the
t(8;21) Fusion Protein
transcription factor complex create dominant inhibitory proteins. However, the mechanisms by which these proteins act remain
obscure. Here we demonstrate that the multidrug resistance 1 (MDR-1)
promoter is a target for AML/ETO transcriptional repression. This
repression is of basal, not activated, expression from the MDR-1
promoter and thus represents a new mechanism for AML/ETO function. We
have defined two domains in AML/ETO that are required for repression of
basal transcription from the MDR-1 promoter: a hydrophobic heptad
repeat (HHR) motif and a conserved zinc finger (ZnF) domain termed the
MYND domain. The HHR mediates formation of AML/ETO homodimers and
AML/ETO-ETO heterodimers. Single serine substitutions at conserved
cysteine residues within the predicted ZnFs also abrogate
transcriptional repression. Finally, we observe that AML/ETO can also
inhibit Ets-1 activation of the MDR-1 promoter, indicating that AML/ETO
can disrupt both basal and Ets-1-dependent transcription. The
fortuitous inhibition of MDR-1 expression in t(8;21)-containing
leukemias may contribute to the favorable response of these patients to
chemotherapeutic drugs.
*
Corresponding author. Mailing address: Department of
Biochemistry and the Vanderbilt Cancer Center, Vanderbilt University School of Medicine, 21st and Garland, Nashville, TN 37027. Phone: (615)
936-3582. Fax: (615) 936-1790. E-mail:
scott.hiebert{at}mcmail.vanderbilt.edu.
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